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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 17, 2015
Inhibition of Notch Signaling During Mouse Incisor Renewal Leads to Enamel DefectsAndrew H Jheon, Michaela Prochazkova, Bo Meng, et al.
Elife|April 29, 2020
Rapamycin rejuvenates oral health in aging miceJonathan Y An, Kristopher A Kerns, Andrew Ouellette, et al.
Anatomical Record (Hoboken, N.J. : 2007)|April 25, 2012
Branch-based model for the diameters of the pulmonary airways: accounting for departures from self-consistency and registration errorsMoni B Neradilek, Nayak L Polissar, Daniel R Einstein, et al.
International Journal of Molecular Sciences|June 27, 2024
Homozygosity for a Rare <i>Plec</i> Variant Suggests a Contributory Role in Congenital Insensitivity to PainPiranit Kantaputra, Teerada Daroontum, Kantapong Kitiyamas, et al.
Cardiovascular Research|February 10, 2015
Impaired myocardial development resulting in neonatal cardiac hypoplasia alters postnatal growth and stress response in the heartJörg-Detlef Drenckhahn, Jette Strasen, Kirsten Heinecke, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 21, 2023
The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4Alana Luzzio, Sarah Edie, Kristina Palmer, et al.
Brain : a Journal of Neurology|July 27, 2012
A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutationsPinki Munot, Dawn E Saunders, Dianna M Milewicz, et al.
International Journal of Molecular Sciences|August 29, 2024
Genetic Variants in the <i>TBC1D2B</i> Gene Are Associated with Ramon Syndrome and Hereditary Gingival FibromatosisThatphicha Kularbkaew, Tipaporn Thongmak, Phan Sandeth, et al.
International Journal of Molecular Sciences|May 25, 2024
Genetic Variants in <i>KCTD1</i> Are Associated with Isolated Dental AnomaliesCholaporn Ruangchan, Chumpol Ngamphiw, Annop Krasaesin, et al.
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